Xanthomonas sp. YL-37의 Alkaline Protease 유전자의 클로닝

Cloning of a Alkaline Protease Gene from Xanthomonas sp. YL-37

  • 이대희 (경남대학교 식품공학과) ;
  • 김수경 (경남대학교 식품공학과) ;
  • 이승철 ;
  • 윤병대 (경남대학교 식품공학과) ;
  • 황용일
  • 발행 : 1995.05.01

초록

For the purpose of developing a new biodegradable detergent, we have isolated a gene encoding wide-range temperature applicable alkaline protease from Xanthomonas sp. YL-37 (Lee et al., 1994, Kor. J. Appl. Microbiol. Biotechnol.). An alkaline protease gene was isolated from the gene bank that was prepared from the chromosomal DNA of Xanthomonas sp. YL-37. From the results of agarose gel electrophoresis and a restriction enzyme mapping, a 2.7 kb DNA fragment containing the alkaline protease gene was inserted in the plasmid pUC9. Extracellular activity of a clone having alkaline protease gene was detected on SDS-polyacrylamide gel with activity staining assay. The molecular weight of alkaline protease was determined to be about 64 kDa from 11% SDS-PAGE analysis. Alkaline protease activity, produced from E. coli which harboring the plasmid, showed no difference at reaction temperature 20, 30 and 40$\circ$C, respectively. This result showed that alkaline protease produced from E. coli harboring the plasmid was apparently the same as that of Xanthomonas sp. YL-37.

키워드

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